Term info
database cross reference
- SCTID:400038003 (MONDO:equivalentTo)
- ICD9:759.7
- Orphanet:93890 (MONDO:equivalentTo)
- NCIT:C99267 (MONDO:equivalentTo)
- UMLS:CN206687 (MONDO:equivalentTo)
- UMLS:C1302790 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
A disease that has its basis in the disruption of embryonic morphogenesis.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_93890, http://linkedlifedata.com/resource/umls/id/CN206687, http://purl.obolibrary.org/obo/NCIT_C99267, http://identifiers.org/snomedct/400038003, http://linkedlifedata.com/resource/umls/id/C1302790
has exact synonym
embryonic morphogenesis disease, rare developmental defect during embryogenesis, malformation syndrome, congenital malformation syndrome, developmental defect during embryogenesis, disorder of embryonic morphogenesis
id
MONDO:0019755